Oxamic acid (High Purity)

CAT:
952-B2010690
Size:
5 g
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Oxamic acid (High Purity) - image 1

Oxamic acid (High Purity)

  • Description:

    Oxamic acid (High Purity)_x000D_ Catalog number: B2010690_x000D_ Lot number: Batch Dependent_x000D_ Expiration Date: Batch dependent_x000D_ Amount: 5 g_x000D_ Molecular Weight or Concentration: 89.05 g/mol_x000D_ Supplied as: Powder_x000D_ Applications: molecular tool for various chemical and biochemical applications_x000D_ Storage: RT_x000D_ Keywords: Oxalic acid monoamide, Aminooxoacetic acid_x000D_ Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ References:_x000D_ 1: Espinoza LC, Sepúlveda P, García A, Martins de Godoi D, Salazar R. Degradation of oxamic_acid using dimensionally stable anodes (DSA) based on a mixture of RuO(2) and IrO(2) nanoparticles Chemosphere. 2020 Jul;251:126674._x000D_ 2: Lan Y, Wang C, Yuan F, Fereja TH, Lou B, Han S, Li J, Xu G. Electrochemiluminescence of 3,4,9,10-perylenetetracarboxylic acid/oxamic hydrazide and its application in the detection of tannic acid Analyst. 2019 Aug 7;144(15):4493-4498._x000D_ 3: Rodríguez-Páez L, Chena-Taboada MA, Cabrera-Hernández A, Cordero-Martínez J, Wong C. Oxamic_acid analogues as LDH-C4-specific competitive inhibitors J Enzyme Inhib Med Chem. 2011 Aug;26(4):579-86._x000D_ 4: Ruddraraju KV, Aggarwal D, Niu C, Baker EA, Zhang RY, Wu L, Zhang ZY. Highly Potent and Selective N-Aryl Oxamic_Acid-Based Inhibitors for Mycobacterium tuberculosis Protein Tyrosine Phosphatase B J Med Chem. 2020 Sep 10;63(17):9212-9227._x000D_ 5: Choi SR, Beeler AB, Pradhan A, Watkins EB, Rimoldi JM, Tekwani B, Avery MA. Generation of oxamic acid libraries: antimalarials and inhibitors of Plasmodium falciparum lactate dehydrogenase J Comb Chem. 2007 Mar-Apr;9(2):292-300._x000D_ 6: Orge CA, Faria JL, Pereira MF. Removal of oxalic acid, oxamic acid and aniline by a combined photolysis and ozonation process Environ Technol. 2015 May-Jun;36(9-12):1075-83._x000D_ 7: Koch RL, Goldman P. The anaerobic metabolism of metronidazole forms N-(2-hydroxyethyl)-oxamic acid J Pharmacol Exp Ther. 1979 Mar;208(3):406-10._x000D_ 8: Yang L, Liu L, Olsen BA, Nussbaum MA. The determination of oxalic acid, oxamic_acid, and oxamide in a drug substance by ion-exclusion chromatography J Pharm Biomed Anal. 2000 Apr;22(3):487-93._x000D_ 9: Aksenov AN, Krayushkin MM, Yarovenko VN. Synthesis of (2-chloroquinolin-3-yl)-1,3,4-thiadiazole-2-carboxamides Russ Chem Bull. 2021;70(6):1131-1134._x000D_ 10: Chiarino D, Grancini G, Frigeni V, Biasini I, Carenzi A. N-(4-Isoxazolylthiazol-2-yl)oxamic acid derivatives as potent orally active antianaphylactic agents J Med Chem. 1991 Feb;34(2):600-5. _x000D_ _x000D_ Products Related to Oxamic acid (High Purity): Chemicals
  • Short Description:

    Catalog Number: B2010690 (5 g)
  • Weight:

    0.8
  • Length:

    2
  • Width:

    0.9
  • Height:

    0.9
  • Height :

    0.9